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If you have enjoyed other solitaire games such as klondike or patience solitaire but are new to Spider Solitaire then you are in for a real treat!

Spider Solitaire is very similar to these other solitaire games and just as fun! There are 10 card foundations, generate 8 stacks of cards with your king through your ace.

If every foundation within the Spider Solitaire game has at least one card then you will have access to additional cards.

To see your additional cards in the Spider Solitaire game simply click on the cards at the bottom right corner of the Spider Solitaire game.

Play Spider Solitaire in several different exciting free web versions! Play with one, two, or four suits!

Once the table is completely empty the game has been won. Spider Solitaire is played with two full decks, cards. At the beginning 54 of the cards are divided between 10 tableaus, the first 4 tableaus have 6 cards each, the other 6 tableaus have 5 cards each.

The top card of each tableau is turned face up, the others are face down. The remaining 50 cards are placed in a stock at the top of the screen.

A card can always be moved onto a card that is one higher in rank. You can for example move a 7 of clubs and put it on an 8 of clubs, or an 8 of hearts, diamonds or spades.

However, even though you can move cards onto other cards in a different suit, the objective of the game is to create runs in the same suit, so a run will only be removed from the table if it's all in the same suit, a full run in different suits doesn't do anything for you.

Although it can be useful to move cards onto other suits just to get them out of the way. You can move multiple cards together if they are all part of a run in the same suit.

However if you have 8 of clubs, 7 of hearts, 6 of diamonds, then you can't move them all together, only the top card. A full run does not have to be the only thing on a tableau to be removed.

For example, a tableau might have three facedown cards and then a full run from King to Ace in the same suit and then the run would disappear, and the three facedown cards would remain.

When there are no more moves that can be made in the tableaus then you can click on the stock in the upper left corner. That will move 10 cards from the stock onto the tableaus, one card onto each tableau.

Game Improvements. Undo Button. Updated Site. Try Something Different. Double Click Feature. Spider Solitaire Social. Spider Solitaire Updates.

Wasp Solitaire. Building the card sequence is done on the columns on the tableau with the foundations not really an active element in the game. You can move revealed cards from the end of the column to another column if you build a valid sequence even from different suits, for example: 7 of spades, 6 of hearts, 5 of spades, 4 of clubs, and 3 of diamonds.

You can also transfer a packed sequence of descending cards as one group to another column if they are from similar suit such as 9 heart, 8 heart, 7 heart on 10 heart or 10 club.

Hence, you can try to pack cards of the same suit if it is allowed, or else you will stuck early on. If you can create a complete sequence of descending cards from King to Ace, then you can move instantly to one foundation.

You can move any card or a sequence of descending cards to empty tableau columns. Once you cannot make any move, you can click on the stock to draw another card to every column on the tableau.

It is a must to fill the empty columns in the tableau before you can draw cards from the stock, even it could break the sequence that you have already created.

It now appears that the spiral orb web may be one of the earliest forms, and spiders that produce tangled cobwebs are more abundant and diverse than orb-web spiders.

The species Bagheera kiplingi was described as herbivorous in , [7] but all other known species are predators , mostly preying on insects and on other spiders, although a few large species also take birds and lizards.

It is estimated that the world's 25 million tons of spiders kill — million tons of prey per year. Most detect prey mainly by sensing vibrations, but the active hunters have acute vision, and hunters of the genus Portia show signs of intelligence in their choice of tactics and ability to develop new ones.

Spiders' guts are too narrow to take solids, so they liquefy their food by flooding it with digestive enzymes.

They also grind food with the bases of their pedipalps , as arachnids do not have the mandibles that crustaceans and insects have. To avoid being eaten by the females, which are typically much larger, male spiders identify themselves to potential mates by a variety of complex courtship rituals.

Males of most species survive a few matings, limited mainly by their short life spans. Females weave silk egg-cases, each of which may contain hundreds of eggs.

Females of many species care for their young, for example by carrying them around or by sharing food with them. A minority of species are social, building communal webs that may house anywhere from a few to 50, individuals.

Social behavior ranges from precarious toleration, as in the widow spiders , to co-operative hunting and food-sharing. While the venom of a few species is dangerous to humans, scientists are now researching the use of spider venom in medicine and as non-polluting pesticides.

Spider silk provides a combination of lightness, strength and elasticity that is superior to that of synthetic materials, and spider silk genes have been inserted into mammals and plants to see if these can be used as silk factories.

As a result of their wide range of behaviors, spiders have become common symbols in art and mythology symbolizing various combinations of patience, cruelty and creative powers.

An abnormal fear of spiders is called arachnophobia. Spiders are chelicerates and therefore arthropods. In fact, chelicerates' only appendages ahead of the mouth are a pair of chelicerae , and they lack anything that would function directly as "jaws".

Spiders and scorpions are members of one chelicerate group, the arachnids. The upper sections generally have thick "beards" that filter solid lumps out of their food, as spiders can take only liquid food.

In spiders, the cephalothorax and abdomen are joined by a small, cylindrical pedicel , which enables the abdomen to move independently when producing silk.

The upper surface of the cephalothorax is covered by a single, convex carapace , while the underside is covered by two rather flat plates.

The abdomen is soft and egg-shaped. It shows no sign of segmentation, except that the primitive Mesothelae , whose living members are the Liphistiidae , have segmented plates on the upper surface.

Like other arthropods, spiders are coelomates in which the coelom is reduced to small areas round the reproductive and excretory systems.

Its place is largely taken by a hemocoel , a cavity that runs most of the length of the body and through which blood flows.

The heart is a tube in the upper part of the body, with a few ostia that act as non-return valves allowing blood to enter the heart from the hemocoel but prevent it from leaving before it reaches the front end.

Hence spiders have open circulatory systems. Spiders have developed several different respiratory anatomies, based on book lungs , a tracheal system, or both.

Mygalomorph and Mesothelae spiders have two pairs of book lungs filled with haemolymph, where openings on the ventral surface of the abdomen allow air to enter and diffuse oxygen.

This is also the case for some basal araneomorph spiders, like the family Hypochilidae , but the remaining members of this group have just the anterior pair of book lungs intact while the posterior pair of breathing organs are partly or fully modified into tracheae, through which oxygen is diffused into the haemolymph or directly to the tissue and organs.

Uniquely among chelicerates , the final sections of spiders' chelicerae are fangs, and the great majority of spiders can use them to inject venom into prey from venom glands in the roots of the chelicerae.

Some pump digestive enzymes from the midgut into the prey and then suck the liquified tissues of the prey into the gut, eventually leaving behind the empty husk of the prey.

Others grind the prey to pulp using the chelicerae and the bases of the pedipalps , while flooding it with enzymes; in these species, the chelicerae and the bases of the pedipalps form a preoral cavity that holds the food they are processing.

The stomach in the cephalothorax acts as a pump that sends the food deeper into the digestive system. The midgut bears many digestive ceca , compartments with no other exit, that extract nutrients from the food; most are in the abdomen, which is dominated by the digestive system, but a few are found in the cephalothorax.

Most spiders convert nitrogenous waste products into uric acid , which can be excreted as a dry material.

Malphigian tubules "little tubes" extract these wastes from the blood in the hemocoel and dump them into the cloacal chamber, from which they are expelled through the anus.

The basic arthropod central nervous system consists of a pair of nerve cords running below the gut, with paired ganglia as local control centers in all segments; a brain formed by fusion of the ganglia for the head segments ahead of and behind the mouth, so that the esophagus is encircled by this conglomeration of ganglia.

Despite the relatively small central nervous system, some spiders like Portia exhibit complex behaviour, including the ability to use a trial-and-error approach.

Spiders have primarily four pairs of eyes on the top-front area of the cephalothorax, arranged in patterns that vary from one family to another.

However, in spiders these eyes are capable of forming images. Unlike the principal eyes, in many spiders these secondary eyes detect light reflected from a reflective tapetum lucidum , and wolf spiders can be spotted by torchlight reflected from the tapeta.

On the other hand, jumping spiders' secondary eyes have no tapeta. Other differences between the principal and secondary eyes are that the latter have rhabdomeres that point away from incoming light, just like in vertebrates, while the arrangement is the opposite in the former.

The principal eyes are also the only ones with eye muscles, allowing them to move the retina. Having no muscles, the secondary eyes are immobile.

Some jumping spiders' visual acuity exceeds by a factor of ten that of dragonflies , which have by far the best vision among insects ; in fact the human eye is only about five times sharper than a jumping spider's.

They achieve this by a telephotographic series of lenses, a four-layer retina and the ability to swivel their eyes and integrate images from different stages in the scan.

The downside is that the scanning and integrating processes are relatively slow. There are spiders with a reduced number of eyes.

Of these, those with six eyes such as Periegops suterii are the most numerous and are missing a pair of eyes on the anterior median line ; [25] other species have four eyes and some just two.

Cave dwelling species have no eyes, or possess vestigial eyes incapable of sight. As with other arthropods, spiders' cuticles would block out information about the outside world, except that they are penetrated by many sensors or connections from sensors to the nervous system.

In fact, spiders and other arthropods have modified their cuticles into elaborate arrays of sensors. Various touch sensors, mostly bristles called setae , respond to different levels of force, from strong contact to very weak air currents.

Chemical sensors provide equivalents of taste and smell , often by means of setae. Males have more chemosensitive bristles on their pedipalps than females.

They have been shown to be responsive to sex pheromones produced by females, both contact and air-borne. Because they are able to tell the sexes apart, it is assumed the blood scent is mixed with pheromones.

In web-building spiders, all these mechanical and chemical sensors are more important than the eyes, while the eyes are most important to spiders that hunt actively.

Like most arthropods, spiders lack balance and acceleration sensors and rely on their eyes to tell them which way is up. Arthropods' proprioceptors , sensors that report the force exerted by muscles and the degree of bending in the body and joints, are well-understood.

On the other hand, little is known about what other internal sensors spiders or other arthropods may have. Each of the eight legs of a spider consists of seven distinct parts.

The part closest to and attaching the leg to the cephalothorax is the coxa ; the next segment is the short trochanter that works as a hinge for the following long segment, the femur ; next is the spider's knee, the patella , which acts as the hinge for the tibia ; the metatarsus is next, and it connects the tibia to the tarsus which may be thought of as a foot of sorts ; the tarsus ends in a claw made up of either two or three points, depending on the family to which the spider belongs.

Although all arthropods use muscles attached to the inside of the exoskeleton to flex their limbs, spiders and a few other groups still use hydraulic pressure to extend them, a system inherited from their pre-arthropod ancestors.

Most spiders that hunt actively, rather than relying on webs, have dense tufts of fine bristles between the paired claws at the tips of their legs.

These tufts, known as scopulae , consist of bristles whose ends are split into as many as 1, branches, and enable spiders with scopulae to walk up vertical glass and upside down on ceilings.

It appears that scopulae get their grip from contact with extremely thin layers of water on surfaces. The abdomen has no appendages except those that have been modified to form one to four usually three pairs of short, movable spinnerets , which emit silk.

Each spinneret has many spigots , each of which is connected to one silk gland.